Canonical Allele Identifier: CA1955232886

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612325G= , CM000673.2:g.17612325G=	GRCh38
NC_000011.9:g.17633872G= , CM000673.1:g.17633872G=	GRCh37
NC_000011.8:g.17590448G=	NCBI36
NG_033191.1:g.69953G=
NG_033191.2:g.69953G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6323G=	ENSP00000382323.2:p.Cys2108=
ENST00000399397.6:c.6287G= MANE Select	ENSP00000382329.2:p.Cys2096=
ENST00000342528.2:c.3341G=	ENSP00000341666.2:p.Cys1114=
ENST00000399391.6:c.6323G=	ENSP00000382323.2:p.Cys2108=
ENST00000399397.5:c.6287G=	ENSP00000382329.2:p.Cys2096=
NM_001277269.1:c.6323G=	NP_001264198.1:p.Cys2108=
NM_001292063.1:c.6287G=	NP_001278992.1:p.Cys2096=
NM_001277269.2:c.6323G=	NP_001264198.1:p.Cys2108=
NM_001292063.2:c.6287G= MANE Select	NP_001278992.1:p.Cys2096=